TRANSFUSION THERAPY IN SPECIAL CONDITIONS Flashcards

(57 cards)

1
Q

Donation of blood by the intended recipient to reduce transfusion reactions and transmission of infectious diseases.

A

Autologous Transfusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

• Blood collected before surgery and stored for later use, either as liquid or frozen.

A

• Predeposit autologous donation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

• Typically reserved for patients anticipating a need for transfusion.

A

• Predeposit autologous donation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

• Collection of blood from the patient before surgery, replaced with fluid, then reinfused at the end of surgery.

A

• Intraoperative hemodilution

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

• Group O RBCs used for patients needing immediate transfusion when ABO and Rh type aren’t known.

A

• Emergency Transfusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

• Group O-negative RBCs preferred for females of childbearing potential.

A

Emergency Transfusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

• Additional blood units selected based on antibody screen after initial transfusion.

A

Emergency Transfusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

• Replacement of one or more blood volumes within 24 hours, usually around 10 units of blood in adults.

A

Massive Transfusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

• Premature infants frequently need RBC transfusions for laboratory tests and to treat anemia.

A

Neonatal Transfusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Neonatal Transfusion
• Dose: [?] with specific considerations for blood units (age, compatibility, CMV status, hemoglobin S).

A

10 mL/kg over 2 to 3 hours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

likely to be required when 30–40% blood volume is lost (approximately 2,000 mL in an adult)

A

Red cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

> 40% blood volume loss is immediately life-threatening.

A

Red cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Pretranfusion compatibility testing should be done early

A

Red cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

It’s best practice to transfuse [?] of the same ABO and RhD group as the patient, however if there are insufficient supplies of the patient’s ABO group available locally, [?] of another ABO compatible group may be released by the Transfusion Service Provider.

A

Red cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

In an emergency situation, uncrossmatched Group O RhD negative red cells (especially for females of childbearing age) may be appropriate.

A

Red cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Should be given through a blood warmer.

A

Red cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

to maintain PT & APTT ≤ 1.5x the normal range, or according to institutional viscoelastic testing algorithm

A

Fresh frozen plasma (FFP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Usual dose is 15 ml/kg.

A

Fresh frozen plasma (FFP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

If the patient’s blood group is unknown, give group AB or group A FFPaccording to jurisdictional guidelines.

A

Fresh frozen plasma (FFP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Allow 1/2 hour thawing time.

A

Fresh frozen plasma (FFP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

• FFP will not provide adequate fibrinogen to correct hypofibrinogenemia in a critically bleeding patient. This should be used.

A

Cryoprecipitate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

• In obstetrics haemorrhage, early DIC is often present so consider it early in this situation.

A

Cryoprecipitate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

• Usual dose is 3–4 g of fibrinogen which is roughly equivalent to 10 units of [?] or 5 units of [?]- your local Transfusion Service Provider can advise on the number of units to provide this dose.

A

whole blood cryoprecipitate

apheresis cryoprecipitate

24
Q

• Allow up to 1/2 hour thawing time.

A

Cryoprecipitate

25
• Thrombocytopenia <50 x 109/L can be anticipated after two blood volume replacementdue to dilution and increased consumption.
Platelets
26
• Aim to keep the platelet count >50 x 109/L (or >100 x 109/L in situations such as CNS injury or diffuse microvascular bleeding).
Platelets
27
• The usual dose in an adultis 1 unit.
Platelets
28
• For life-threatening (critical organ) and clinically significant bleeds, the consensus is to use a combination of.
Prothrombinex-VF, Vitamin K and FFP
29
• Vitamin K1:
5–10 mg IV
30
• Prothrombinex (PTX-VF):
50 IU/kg
31
• Fresh frozen plasma: [?] if Prothrombinex-VF not available
150–300 mL or 15 mL/kg
32
• Note that the use of blood components in patients with critical bleeding is lifesaving, but increased volumes may be independently associated with
mortality and ARDS.
33
• [?] on specimen tubes compared to patient’s hospital armband at bedside to prevent mislabeling. • [?] applied to tubes before leaving bedside to avoid errors.
Labels
34
require sterile, pyrogen-free transfusion sets with filters designed to retain harmful particles.
AABB standards
35
• Blood components infused slowly for [?], with close observation for reactions.
10-15 minutes
36
• Subsequent infusion should be as rapid as tolerated, ideally within [?].
4 hours
37
• Standard sets include a [?] to remove gross clots and cellular debris.
150-260 μm filter
38
• Mandatory use of [?] for all blood component transfusions.
blood administration filter
39
• Current good manufacturing practice (cGMP) regulations set by the FDA govern the entire process of blood component management, from receipt to transfusion.
cGMP Regulations
40
• These regulations provide standards for the collection, processing, storage, and distribution of blood and blood components.
cGMP Regulations
41
• Compliance with cGMP regulations is essential to maintain the quality, purity, and potency of blood products, minimizing the risk of adverse events during transfusion.
cGMP Regulations
42
• Each blood product is prepared and stored under specific conditions to preserve its purity and potency until the time of transfusion.
Optimizing Purity and Potency
43
• Proper storage temperatures and conditions are maintained to prevent degradation of components and ensure their efficacy.
Optimizing Purity and Potency
44
• Techniques such as leukoreduction (removal of white blood cells) and irradiation may be employed to enhance the safety and quality of blood components.
Optimizing Purity and Potency
45
1.Quality control parameters are established by regulatory bodies like the FDA and professional organizations like AABB.
Quality Control
46
2.These parameters encompass various aspects of blood component management, including collection methods, processing techniques, storage conditions, and testing protocols.
Quality Control
47
3.Regular quality control checks and audits are conducted to monitor compliance with established standards and identify any deviations that may affect product quality or patient safety.
Quality Control
48
1.Component indications refer to specific guidelines and criteria for the selection and transfusion of different blood components based on patient needs and clinical indications.
Component Indications
49
2.Indications help healthcare providers make informed decisions regarding the use of whole blood, packed red blood cells, platelets, plasma, and other blood products.
Component Indications
50
3.Adhering to component indications minimizes the risk of adverse transfusion reactions, such as hemolytic reactions, transfusionrelated acute lung injury (TRALI), and transfusion-associated circulatory overload (TACO).
Component Indications
51
4.Indications may include factors such as patient diagnosis, hemoglobin level, platelet count, coagulation profile, and specific clinical scenarios (e.g., massive transfusion, neonatal transfusion).
Component Indications
52
• A single unit of packed red blood cells (pRBCs) is usually infused over 1 to 4 hours, depending on the transfusion rate and the patient's tolerance.
Red Blood Cell (RBC) Transfusion:
53
• Multiple units of pRBCs may be administered sequentially, extending the overall duration of the transfusion session.
Red Blood Cell (RBC) Transfusion:
54
• Platelet transfusions are typically infused over 30 to 60 minutes per unit, but the duration may vary based on institutional protocols and patient factors.
Platelet Transfusion:
55
1.Fresh frozen plasma (FFP) or other plasma components are generally infused over 30 to 60 minutes per unit.
Plasma Transfusion
56
2.Additional plasma products, such as cryoprecipitate or prothrombin complex concentrate (PCC), may also be administered, each with its own infusion duration.
Plasma Transfusion
57
1.Whole blood transfusions, while less common than component transfusions, are typically infused over 1 to 4 hours, similar to pRBC transfusions.
Whole Blood Transfusion: